# K243940: VITA YZ Multi Translucent

- Pathway: 510(k) (Traditional)
- Applicant: Vita Zahnfabrik H.Rauter GmbH & Co.
- Decided: Feb 21, 2025 after 63 days
- Product code: EIH (Powder, Porcelain)
- Device class: 2
- Regulation: 21 CFR 872.6660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K920425 (1992). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180703: VITA YZ ST and VITA YZ XT, Vita Zahnfabrik H.Rauter GmbH Co. (2018)
- K122269: Enamic, Vita Zahnfabrik H.Rauter GmbH & Co. (2012) Summary page 5.

## Indications for use
VITAYZ MULTI TRANSLUCENT is indicated for: fully anatomical anterior and posterior crowns fully anatomical 4 unit anterior and posterior bridges fully and partially veneered single tooth and up to 4-unit bridge substructures in the anterior and posterior tooth regions inlays Onlays veneers

Source page: https://510kreport.com/device/K243940
Methodology: https://510kreport.com/methodology